HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 5-Acetoxy-4,6-di-tert-butylbenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | 4-Acetoxy-3,5-di-tert-butyl-2-formylmethylanisole | HCID 10881749 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Acetoxy-4,6-di-tert-butylbenzofuran | HCID 11822332 | — |
Reaction Steps
4-Acetoxy-3,5-di-tert-butyl-2-formylmethylanisole (16 g) was dissolved in dichloromethane (100 ml) and trimethylsilyl iodide (7.1 ml) was added dropwise to the solution under cooling with ice. After stirring the mixture at room temperature for 1 h, a saturated aqueous solution of sodium thiosulfate was added and the mixture was subjected to extraction with chloroform. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 5-acetoxy-4,6-di-tert-butylbenzofuran quantitatively (14.3 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05606089 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-e86e90d95a5e4978a694c46c5685407a |
| Source note | uspto-grants-1997_02 |